On the one hand, professional rules of conduct are designed to preserve the traditional vision, but, on the other hand, those rules are
created by regulatory bodies dominated by corporate practitioners.
Not exact matches
What we do really encompasses every bit of the clinical development process — from early clinical development when compounds are
created, to running clinical trials, to conducting post-approval studies after the drug has been approved
by the Food and Drug Association (FDA) or a similar
regulatory body outside of the US.
They organized themselves and took responsibility for their industry's results; got ahead of the
regulatory bodies; and shaped their own destiny
by deploying common quality practices and
creating outcome - based standards.
Hospitals have always disclosed information but the big shift is that with FIPPA it has
created a statutory and
regulatory regime for requests, setting out exclusions and a time period for processing requests, a way of calculating costs, and an independent
body in the form of the information privacy commissioner reviewing decisions made
by hospitals.
The core essence of «trust» —
created today with government guarantees, physical vaults, behemoth balance sheets to make institutions seemingly «too big to fail», and layer upon layer of
regulatory framework enforced
by «zillions» (yes I know its not a real number and not an accurate one, but there's no way for me to count the
bodies spending time making banks function) of people leading very exciting lives holding a gigantic ball of water in the air — is likely on the front edge of a very big wave of foundational change.